Data Management STREAM

  1. Navigating Trials With Confidence: Building A Robust External Control Arm 12/21/2023

    Explore methods to build scientifically rigorous comparator groups to allow more patients access to life-saving treatments, accelerate trial timelines, and maximize resources.

  2. Verana Health: Where Quality Powers Insights 5/28/2025

    Drive innovation by improving your digital health in ophthalmology, urology, and neurology. 

  3. Evolving Data Review With AI 2/25/2025

    AI is transforming clinical data review by automating processes and enhancing efficiency. Discover the four stages of evolution that emphasize automation, regulatory alignment, data analysis, and human oversight.

  4. Clinical Analytics Use Cases For AI 2/25/2025

    Automating FDA data validation rules and analyzing audit trail data can significantly reduce fraud and predict areas of concern. Discover how these advancements can transform your clinical trials.

  5. How To Boost Disclosure Efficiencies With Outsourcing 11/1/2018

    In this webinar, you’ll hear about exciting new advisory and managed disclosure services from TrialScope, including: compliance, policy and process assessments, as well as plain-language summaries, protocol registration, results posting, and redaction services.

  6. Addressing Opportunities And Challenges In Digital Health Data 10/22/2024

    Experts from diverse industry sectors unpack key points from the FDA’s final guidance on Digital Health Technologies (DHT) for remote data collection in clinical investigations.

  7. Manage Exponential Data Growth With Medidata Clinical Data Studio 6/19/2025

    Bring study teams together like never before for total data quality oversight.

  8. Importance And Requirements Of Study Results Posting 1/15/2020

    In addition to laws requiring disclosure of clinical trial results, the public also demands this information. TrialScope Chief Strategy Officer Thomas Wicks explains why sponsors should share study results.

  9. Streamline EDC Data Entry Using EHR Data 1/17/2023

    Explore how a clinical research coordinator (CRC) typically manually re-enters data from their EHR/EMR system into Rave EDC, and how Rave Companion provides automated assistance to enable the CRC to complete EDC forms.

  10. Global Compliance Made Easy 5/6/2019

    Global clinical trial disclosure compliance is inherently complex, with over 39 registries, Most sponsors simply lack visibility into all the places they need to disclose information or what their commitments are. Automation can help make global compliance easier.